[go: up one dir, main page]

TR200201014T2 - Heterocyclic sodium / proton exchange inhibitors and method - Google Patents

Heterocyclic sodium / proton exchange inhibitors and method

Info

Publication number
TR200201014T2
TR200201014T2 TR2002/01014T TR200201014T TR200201014T2 TR 200201014 T2 TR200201014 T2 TR 200201014T2 TR 2002/01014 T TR2002/01014 T TR 2002/01014T TR 200201014 T TR200201014 T TR 200201014T TR 200201014 T2 TR200201014 T2 TR 200201014T2
Authority
TR
Turkey
Prior art keywords
proton exchange
heterocyclic
sodium
heteroaryl
exchange inhibitors
Prior art date
Application number
TR2002/01014T
Other languages
Turkish (tr)
Inventor
Ahmad Saleem
C.Wu Shung
V.O'neil Steven
Ngu Khehyong
S. Atwal Karnail
S.Weinstein David
Original Assignee
Bristol-Myers Squibb Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol-Myers Squibb Company filed Critical Bristol-Myers Squibb Company
Publication of TR200201014T2 publication Critical patent/TR200201014T2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/88Nitrogen atoms, e.g. allantoin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms
    • C07D239/49Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/38Nitrogen atoms
    • C07D277/40Unsubstituted amino or imino radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/08Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/08Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing alicyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/08Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Obesity (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Emergency Medicine (AREA)
  • Vascular Medicine (AREA)
  • Psychiatry (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

n'nin 1 ila 5 arasinda oldugu; X'in N ya da C-R5(ki buradaki R5, H, halo, alkenil,alkinil, alkoksi, alkil, aril ya da heteroarildir) oldugu; Z'nin bir heteroaril grubu oldugu; R , R , R ve R4'ün burada tanimlandigi gibi oldugu ve X'in N, R 'in tercihen aril ya da heteroaril oldugu yapi (I)'e sahip sodyum/proton degisim (NHE) önleyicileri olan heterosiklik saglanmistir ve bunlari, antianjinal ve kardiyo koruyucu maddeler olarak faydalidir. Ayrica anjin pektoris, kardiyak fonksiyonsuzluk, miyokardiyal nekroz ve aritmanin önlenmesi ya da tedavi edilmesine yönelik, yukaridaki heterosiklik türevlerin kullanildigi bir metot da saglanmistir.n is from 1 to 5; X is N or C-R5 (wherein R5 is H, halo, alkenyl, alkynyl, alkoxy, alkyl, aryl, or heteroaryl); Z is a heteroaryl group; Heterocyclic is provided, which are sodium / proton exchange (NHE) inhibitors having structure (I) where R, R, R and R4 are as defined herein and X is N, R is preferably aryl or heteroaryl. and it is useful as cardio preservatives. Also provided is a method for the prevention or treatment of angina pectoris, cardiac dysfunction, myocardial necrosis and arrhythmia using the above heterocyclic derivatives.

TR2002/01014T 1999-10-12 2000-10-02 Heterocyclic sodium / proton exchange inhibitors and method TR200201014T2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15875599P 1999-10-12 1999-10-12

Publications (1)

Publication Number Publication Date
TR200201014T2 true TR200201014T2 (en) 2003-01-21

Family

ID=22569562

Family Applications (1)

Application Number Title Priority Date Filing Date
TR2002/01014T TR200201014T2 (en) 1999-10-12 2000-10-02 Heterocyclic sodium / proton exchange inhibitors and method

Country Status (26)

Country Link
US (2) US6887870B1 (en)
EP (1) EP1224183B1 (en)
JP (1) JP2003527331A (en)
KR (1) KR20020038818A (en)
CN (1) CN1468232A (en)
AR (1) AR026023A1 (en)
AT (1) ATE314364T1 (en)
AU (1) AU7859600A (en)
BR (1) BR0014725A (en)
CA (1) CA2388813A1 (en)
CO (1) CO5251416A1 (en)
DE (1) DE60025245T2 (en)
DK (1) DK1224183T3 (en)
ES (1) ES2254236T3 (en)
HK (1) HK1045691A1 (en)
HU (1) HUP0300195A3 (en)
IL (1) IL148517A0 (en)
MX (1) MXPA02003626A (en)
NO (1) NO20021717L (en)
NZ (1) NZ517668A (en)
PE (1) PE20011001A1 (en)
PL (1) PL366131A1 (en)
RU (1) RU2002111867A (en)
TR (1) TR200201014T2 (en)
WO (1) WO2001027107A2 (en)
ZA (1) ZA200202479B (en)

Families Citing this family (75)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6667344B2 (en) 2001-04-17 2003-12-23 Dey, L.P. Bronchodilating compositions and methods
US20030055026A1 (en) 2001-04-17 2003-03-20 Dey L.P. Formoterol/steroid bronchodilating compositions and methods of use thereof
US7217701B2 (en) 2001-10-11 2007-05-15 Katsuhiko Mikoshiba Intracellular calcium concentration increase inhibitors
US20060013775A1 (en) * 2001-11-26 2006-01-19 Gristwood Robert W Use of ppar activators for the treatment of pulmonary fibrosis
WO2004022536A1 (en) * 2002-09-04 2004-03-18 Glenmark Pharmaceuticals Limited New heterocyclic amide compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them
AU2003269317B2 (en) 2002-10-23 2009-10-29 Glenmark Pharmaceuticals Ltd. Novel tricyclic compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them
AU2003292039A1 (en) 2002-11-18 2004-06-15 Novartis Ag Imidazo(1, 5a)pyridine derivatives and methods for treating aldosterone mediated diseases
NZ540612A (en) * 2003-01-14 2008-02-29 Arena Pharm Inc 1,2,3-Trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia
SI1599468T1 (en) * 2003-01-14 2008-02-29 Arena Pharm Inc 1,2,3-trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia
EP1862181A3 (en) * 2003-04-11 2010-09-15 High Point Pharmaceuticals, LLC New pyrazolo[1,5-a] pyrimidine derivatives and pharmaceutical use thereof
WO2004089940A1 (en) 2003-04-11 2004-10-21 Glenmark Pharmaceuticals S.A. Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them
AU2003901812A0 (en) * 2003-04-15 2003-05-01 Vital Health Sciences Pty Ltd Phosphates of secondary alcohols
US8026264B2 (en) * 2003-05-29 2011-09-27 Merck Sharp And Dohme Corp. Triazole derivatives as inhibitors of 11-β hydroxysteroid dehydrogenase-1
GB0315950D0 (en) 2003-06-11 2003-08-13 Xention Discovery Ltd Compounds
TWI359675B (en) 2003-07-10 2012-03-11 Dey L P Bronchodilating β-agonist compositions
AR045047A1 (en) * 2003-07-11 2005-10-12 Arena Pharm Inc ARILO AND HETEROARILO DERIVATIVES TRISUSTITUIDOS AS MODULATORS OF METABOLISM AND PROFILAXIS AND TREATMENT OF DISORDERS RELATED TO THEMSELVES
EA010023B1 (en) 2003-07-14 2008-06-30 Арена Фармасьютикалз, Инк. Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto
ATE430741T1 (en) 2003-07-24 2009-05-15 Euro Celtique Sa PIPERIDINE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
US8455489B2 (en) * 2003-11-10 2013-06-04 Exelixis, Inc. Substituted pyrimidine compositions and methods of use
US8519158B2 (en) * 2004-03-12 2013-08-27 Ligand Pharmaceuticals Incorporated Androgen receptor modulator compounds and methods
GB0412986D0 (en) 2004-06-10 2004-07-14 Xention Discovery Ltd Compounds
JP2009519206A (en) 2004-10-13 2009-05-14 グレンマーク・ファーマシューティカルズ・エスエー Process for producing N- (3,5-dichloropyridin-4-yl) -4-difluoromethoxy-8-methanesulfonamido-dibenzo [B, D] furan-1-carboxamide
US7576212B2 (en) 2004-12-09 2009-08-18 Xention Limited Thieno[2,3-B] pyridines as potassium channel inhibitors
AR066386A1 (en) 2004-12-17 2009-08-19 Glenmark Pharmaceuticals Sa CONDENSED HETEROCICLICAL COMPOUNDS, METHODS AND INTERMEDIARIES FOR THEIR PREPARATION, A PHARMACEUTICAL COMPOSITION THAT INCLUDES THEM AND THEIR USE IN THE TREATMENT OF DISEASES MEDIATED BY THE INHIBITION OF PDE-4
ES2417491T3 (en) 2004-12-17 2013-08-08 Glenmark Pharmaceuticals S.A. Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders
US7807691B2 (en) 2005-05-13 2010-10-05 Eli Lilly And Company Substituted N-arylpyrrolidines as selective androgen receptor modulators
GB0525164D0 (en) 2005-12-09 2006-01-18 Xention Discovery Ltd Compounds
EP2479173A1 (en) 2007-04-27 2012-07-25 Purdue Pharma LP Therapeutic agents useful for treating pain
TWI362930B (en) 2007-04-27 2012-05-01 Purdue Pharma Lp Trpv1 antagonists and uses thereof
CN101679191B (en) 2007-06-05 2014-03-12 塞诺菲-安万特股份有限公司 Di(hetero)arylcyclohexane derivatives, their preparation, their use and pharmaceutical compositions comprising them
GB0818241D0 (en) * 2008-10-06 2008-11-12 Cancer Res Technology Compounds and their use
US8759362B2 (en) * 2008-10-24 2014-06-24 Purdue Pharma L.P. Bicycloheteroaryl compounds and their use as TRPV1 ligands
US8703962B2 (en) * 2008-10-24 2014-04-22 Purdue Pharma L.P. Monocyclic compounds and their use as TRPV1 ligands
WO2018129556A1 (en) 2017-01-09 2018-07-12 Ardelyx, Inc. Compounds and methods for inhibiting nhe-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
SI2384318T1 (en) 2008-12-31 2018-03-30 Ardelyx, Inc. Compounds and methods for inhibiting nhe-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
JP5876423B2 (en) 2010-06-22 2016-03-02 塩野義製薬株式会社 Compounds having TRPV1 inhibitory activity and uses thereof
CN103221410B (en) 2010-09-22 2017-09-15 艾尼纳制药公司 GPR119 receptor modulators and treatment of disorders associated therewith
GB201105659D0 (en) 2011-04-01 2011-05-18 Xention Ltd Compounds
KR20140007954A (en) * 2011-06-10 2014-01-20 메르크 파텐트 게엠베하 Compositions and methods for the production of pyrimidine and pyridine compounds with btk inhibitory activity
KR101589837B1 (en) 2011-06-22 2016-01-29 퍼듀 퍼머 엘피 Trpv1 antagonists including dihydroxy substituent and uses thereof
US9394293B2 (en) 2011-08-10 2016-07-19 Purdue Pharma L.P. TRPV1 antagonists including dihydroxy substituent and uses thereof
AR090037A1 (en) 2011-11-15 2014-10-15 Xention Ltd DERIVATIVES OF TIENO AND / OR FURO-PYRIMIDINES AND PYRIDINES INHIBITORS OF THE POTASSIUM CHANNELS
US8765959B2 (en) * 2011-12-23 2014-07-01 Boehringer Ingelheim International Gmbh Piperidine derivatives
TWI598099B (en) * 2012-04-30 2017-09-11 健生科學愛爾蘭無限公司 New compounds and new use
PE20142366A1 (en) * 2012-05-30 2015-01-10 Hoffmann La Roche TRIAZOLO COMPOUNDS AS PDE INHIBITORS 10
WO2014010748A1 (en) * 2012-07-10 2014-01-16 Shionogi & Co., Ltd. Cyclopropane derivative having bace1 inhibiting activity
JP6009851B2 (en) * 2012-07-27 2016-10-19 日本曹達株式会社 Method for producing 1H-tetrazole derivative
US10376481B2 (en) 2012-08-21 2019-08-13 Ardelyx, Inc. Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
RU2015107019A (en) 2012-08-21 2016-10-10 Эрделикс Инк. COMPOUNDS AND METHODS FOR INHIBITING AN NHE-MEDIATED ANTI-PORT IN THE TREATMENT OF DISORDERS ASSOCIATED WITH DELAY OF LIQUID OR SALT OVERLOAD AND DISEASES OF THE GASTROINTESTINAL TRACT
US8652527B1 (en) 2013-03-13 2014-02-18 Upsher-Smith Laboratories, Inc Extended-release topiramate capsules
US9101545B2 (en) 2013-03-15 2015-08-11 Upsher-Smith Laboratories, Inc. Extended-release topiramate capsules
MX382203B (en) 2013-04-12 2025-03-11 Ardelyx Inc NHE3 (SODIUM-HYDROGEN EXCHANGER 3) BINDING COMPOUNDS AND METHODS FOR INHIBITING PHOSPHATE TRANSPORT.
EP4445956A3 (en) 2015-01-06 2024-12-04 Arena Pharmaceuticals, Inc. Compound for use in treating conditions related to the s1p1 receptor
PL3310760T3 (en) 2015-06-22 2023-03-06 Arena Pharmaceuticals, Inc. Crystalline l-arginine salt of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclo-penta[b]indol-3-yl)acetic acid for use in s1p1 receptor-associated disorders
HUE057460T2 (en) 2016-03-22 2022-05-28 Merck Sharp & Dohme Allosteric modulators of nicotinic acetylcholine receptors
RU2741911C2 (en) 2016-04-29 2021-01-29 Иомет Фарма Лтд. New substituted imidazopyridine compounds as indoleamine-2,3-dioxygenase and/or tryptophan-2,3-dioxygenase inhibitors
JP2020505333A (en) 2017-01-09 2020-02-20 アルデリックス, インコーポレイテッド Inhibitors of NHE-mediated antiport
UA126283C2 (en) 2017-01-09 2022-09-14 Арделікс, Інк. COMPOUNDS USEFUL FOR THE TREATMENT OF DISORDERS OF THE GASTROINTESTINAL TRACT
MA47504A (en) 2017-02-16 2019-12-25 Arena Pharm Inc COMPOUNDS AND TREATMENT METHODS FOR PRIMITIVE BILIARY ANGIOCHOLITIS
WO2018149940A1 (en) 2017-02-17 2018-08-23 Quimica Sintetica, S. A. Process for the preparation of enantiomerically enriched dihydrobenzofurans and intermediate compounds obtained in the process
WO2018224455A1 (en) 2017-06-07 2018-12-13 Basf Se Substituted cyclopropyl derivatives
WO2018234488A1 (en) 2017-06-23 2018-12-27 Basf Se SUBSTITUTED CYCLOPROPYL DERIVATIVES
KR20240144491A (en) 2017-08-04 2024-10-02 알데릭스, 인코포레이티드 Glycyrrhetinic acid derivatives for treating hyperkalemia
WO2019121143A1 (en) 2017-12-20 2019-06-27 Basf Se Substituted cyclopropyl derivatives
US20220324835A1 (en) * 2018-01-26 2022-10-13 Nurix Therapeutics, Inc. Inhibitors of cbl-b and methods of use thereof
JP7590183B2 (en) 2018-03-13 2024-11-26 武田薬品工業株式会社 Substituted imidazopyridines as inhibitors of plasma kallikrein and their uses
ES2987794T3 (en) 2018-06-06 2024-11-18 Arena Pharm Inc Treatment procedures for S1P1 receptor-related conditions
EP4234016B1 (en) 2019-02-07 2025-06-18 Ardelyx, Inc. Glycyrrhetinic acid derivatives for use in treating hyperkalemia
CN114364667B (en) 2019-04-09 2025-01-10 紐力克斯治疗公司 3-Substituted piperidine compounds for Cbl-b inhibition and use of Cbl-b inhibitors in combination with cancer vaccines and/or oncolytic viruses
BR112021020864A2 (en) 2019-04-19 2021-12-14 Ligand Pharm Inc Crystalline forms and methods of producing crystalline forms of a compound
WO2020237096A1 (en) 2019-05-21 2020-11-26 Ardelyx, Inc. Combination for lowering serum phosphate in a patient
EP4031245A1 (en) 2019-09-18 2022-07-27 Takeda Pharmaceutical Company Limited Heteroaryl plasma kallikrein inhibitors
EP4477220A3 (en) 2019-09-18 2025-02-26 Takeda Pharmaceutical Company Limited Plasma kallikrein inhibitors and uses thereof
US20230382891A1 (en) * 2020-10-20 2023-11-30 Blacksmith Medicines, Inc. Glutaminyl-peptide cyclotransferase like (qpctl) protein inhibitors and uses thereof
CN117396474A (en) * 2021-03-17 2024-01-12 武田药品工业株式会社 Plasma kallikrein inhibitors

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1206498B (en) 1983-07-18 1989-04-27 Angeli Inst Spa AMIDINE DERIVATIVES OF 4-PHENYLMIDAZOLE 2-SUBSTITUTE PROCESSES FOR THEIR PREPARATION AND THEIR PHARMACEUTICAL USE.
FR2579596B1 (en) * 1985-03-26 1987-11-20 Inst Nat Sante Rech Med (IMIDAZOLYL-4) PIPERIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
IT1201454B (en) * 1985-08-19 1989-02-02 Boehringer Biochemia Srl 1,4-dihydropyridine-2-SUBSTITUTED
US4663473A (en) * 1986-08-25 1987-05-05 The United States Of America As Represented By The Secretary Of The Army Isocyanates from oxalyl chloride and amines
FR2674855B1 (en) * 1991-04-03 1994-01-14 Synthelabo PIPERIDINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION.
US5380858A (en) * 1992-04-01 1995-01-10 The University Of Toledo Process for the preparation of intermediates useful for the synthesis of histamine receptor antagonists
FR2696177B1 (en) * 1992-09-28 1995-05-12 Synthelabo Piperidine derivatives, their preparation and their therapeutic application.
NZ326354A (en) * 1996-01-15 1999-05-28 Janssen Pharmaceutica Nv 3-(substituted-1-piperazinyl)-6-(substituted-1,2,4-thiadiazol-5 -yl)-pyridazine derivatives and medicaments
FR2765221B1 (en) 1997-06-25 1999-07-30 Synthelabo DERIVATIVES OF 4 - [(1H-IMIDAZOL-4-YL) PIPERIDIN-1-YL] ANILIDE, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
FR2765580B1 (en) 1997-07-01 1999-08-06 Synthelabo (1H-IMIDAZOL-4-YL) PIPERIDINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
FR2772377B1 (en) * 1997-12-12 2000-01-07 Synthelabo DERIVATIVES OF 1- (1-H-IMIDAZOL-2-YL) PYRROLIDINES AND 1- (1-H-IMIDAZOL-2-YLPIPERIDINES), THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
US6011059A (en) * 1997-12-24 2000-01-04 Bristol-Myers Squibb Company Acyl guanidine sodium/proton exchange inhibitors and method
EP1136489A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-[Piperidin-1-yl]pyrimidone derivatives

Also Published As

Publication number Publication date
CN1468232A (en) 2004-01-14
RU2002111867A (en) 2004-05-10
PL366131A1 (en) 2005-01-24
IL148517A0 (en) 2002-09-12
DE60025245T2 (en) 2006-08-24
PE20011001A1 (en) 2001-11-25
HK1045691A1 (en) 2002-12-06
AU7859600A (en) 2001-04-23
ZA200202479B (en) 2004-10-27
AR026023A1 (en) 2002-12-26
MXPA02003626A (en) 2003-09-22
US20050137216A1 (en) 2005-06-23
ATE314364T1 (en) 2006-01-15
WO2001027107A2 (en) 2001-04-19
NO20021717L (en) 2002-06-10
CA2388813A1 (en) 2001-04-19
WO2001027107A3 (en) 2002-01-24
HUP0300195A3 (en) 2003-09-29
EP1224183A2 (en) 2002-07-24
ES2254236T3 (en) 2006-06-16
KR20020038818A (en) 2002-05-23
BR0014725A (en) 2003-06-17
NZ517668A (en) 2004-09-24
HUP0300195A2 (en) 2003-07-28
DK1224183T3 (en) 2006-03-06
US7326705B2 (en) 2008-02-05
CO5251416A1 (en) 2003-02-28
EP1224183B1 (en) 2005-12-28
US6887870B1 (en) 2005-05-03
DE60025245D1 (en) 2006-02-02
JP2003527331A (en) 2003-09-16
NO20021717D0 (en) 2002-04-11

Similar Documents

Publication Publication Date Title
TR200201014T2 (en) Heterocyclic sodium / proton exchange inhibitors and method
MXPA02003977A (en) INHIBITORS OF agr;L.
DE60008352D1 (en) PYRIDOXINE DERIVATIVES IN THE TREATMENT OF CARDIOVASCULAR COMPLAINTS
AU2019502A (en) Anilinopyrimidine derivatives as ikk inhibitors and compositions and methods related thereto
WO2003050261A3 (en) (1-phenyl-2-heteroaryl)ethyl-guanidine compounds as inhibitors of mitochondrial f1f0 atp hydrolase
AP1902A (en) N-aryl-2-oxazolidinone-5-carboxamides and their derivatives and their use as antibacterials
ATE241621T1 (en) ARYLSULFONYLS AS FACTOR XA INHIBITORS
EA200200374A1 (en) QUINOLYLPROPYLPIPERIDINE DERIVATIVES, THEIR RECEIVING AND THE CONTAINING COMPOSITIONS
ATE309237T1 (en) AROMATIC HETEROCYCLIC COMPOUNDS AS ANTI-INFLAMMATORY ACTIVES
NO20003111D0 (en) Ortho-anthranilamide derivatives as anticoagulants
MY142109A (en) Pyrimidine derivatives for the treatment of abnormal cell growth
ATE290382T1 (en) HETEROCYCLIC POTASSIUM CHANNEL INHIBITORS
EA200200301A1 (en) SUBSTITUTED COLLECTION CENTER
NO984740L (en) Isatin derivatives such as acetylcholinesterase inhibitors and analgesics
TR200403436T2 (en) Crystalline 1-methylcarbapenem derivatives.
AU2492500A (en) Aspartic protease inhibitors, compositions, and associated therapeutic methods
BR0014990A (en) Ranphthalazinone tetrahydrothiopyrane derivatives as pde4 inhibitors
YU30603A (en) Bridged piperazine derivatives
CA2191947A1 (en) Pirydyl Imidazole Derivatives and Processes for the Preparation Thereof
DE60105618D1 (en) DIHYDROPORPHYRINE DERIVATIVES AND THEIR USE
DE60043228D1 (en) PREPARATION OF 2-CYANOPYRIDINES
ATE261973T1 (en) MICROBICIDAL EFFECT OF PORPHYRINS IN THE DARK
DE59803066D1 (en) SUBSTITUTED BENZYLOXYIMINO COMPOUNDS
ATE279113T1 (en) HYPOXANTHINE AND THIOHYPXANTHINE COMPOUNDS
ECSP982799A (en) SODIUM INHIBITORS EXCHANGE OF ACIL GUANIDINE PROTONS AND METHOD OF USE